1. A Wave of Regulatory T Cells into Neonatal Skin Mediates Tolerance to Commensal Microbes
- Author
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Scharschmidt, Tiffany C, Vasquez, Kimberly S, Truong, Hong-An, Gearty, Sofia V, Pauli, Mariela L, Nosbaum, Audrey, Gratz, Iris K, Otto, Michael, Moon, James J, Liese, Jan, Abbas, Abul K, Fischbach, Michael A, and Rosenblum, Michael D
- Subjects
Biomedical and Clinical Sciences ,Immunology ,Pediatric ,Microbiome ,Infectious Diseases ,1.1 Normal biological development and functioning ,2.1 Biological and endogenous factors ,Inflammatory and immune system ,Good Health and Well Being ,Animals ,Animals ,Newborn ,Antigens ,Bacterial ,Host-Pathogen Interactions ,Immune Tolerance ,Inflammation ,Mice ,Mice ,Inbred C57BL ,Microbiota ,Molecular Sequence Data ,Skin ,Staphylococcal Infections ,Staphylococcus epidermidis ,T-Lymphocytes ,Regulatory - Abstract
The skin is a site of constant dialog between the immune system and commensal bacteria. However, the molecular mechanisms that allow us to tolerate the presence of skin commensals without eliciting destructive inflammation are unknown. Using a model system to study the antigen-specific response to S. epidermidis, we demonstrated that skin colonization during a defined period of neonatal life was required for establishing immune tolerance to commensal microbes. This crucial window was characterized by an abrupt influx of highly activated regulatory T (Treg) cells into neonatal skin. Selective inhibition of this Treg cell wave completely abrogated tolerance. Thus, the host-commensal relationship in the skin relied on a unique Treg cell population that mediated tolerance to bacterial antigens during a defined developmental window. This suggests that the cutaneous microbiome composition in neonatal life is crucial in shaping adaptive immune responses to commensals, and disrupting these interactions might have enduring health implications.
- Published
- 2015